CN100513485C - 电极电路保护用硅橡胶组合物、电极电路保护材料和电气、电子零件 - Google Patents
电极电路保护用硅橡胶组合物、电极电路保护材料和电气、电子零件 Download PDFInfo
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- CN100513485C CN100513485C CNB2004100852991A CN200410085299A CN100513485C CN 100513485 C CN100513485 C CN 100513485C CN B2004100852991 A CNB2004100852991 A CN B2004100852991A CN 200410085299 A CN200410085299 A CN 200410085299A CN 100513485 C CN100513485 C CN 100513485C
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- silicone rubber
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- 229920002379 silicone rubber Polymers 0.000 title claims abstract description 84
- 239000004945 silicone rubber Substances 0.000 title claims abstract description 76
- 239000000463 material Substances 0.000 title claims description 8
- 229910001410 inorganic ion Inorganic materials 0.000 claims abstract description 13
- 229920001296 polysiloxane Polymers 0.000 claims description 40
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- 125000003342 alkenyl group Chemical group 0.000 claims description 26
- 239000003054 catalyst Substances 0.000 claims description 19
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 15
- 229920006136 organohydrogenpolysiloxane Polymers 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
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- 238000006482 condensation reaction Methods 0.000 claims description 9
- 239000007809 chemical reaction catalyst Substances 0.000 claims description 8
- 150000001451 organic peroxides Chemical class 0.000 claims description 8
- 239000003999 initiator Substances 0.000 claims description 7
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 4
- 229910052787 antimony Inorganic materials 0.000 claims description 4
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 4
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
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- UMHKOAYRTRADAT-UHFFFAOYSA-N [hydroxy(octoxy)phosphoryl] octyl hydrogen phosphate Chemical compound CCCCCCCCOP(O)(=O)OP(O)(=O)OCCCCCCCC UMHKOAYRTRADAT-UHFFFAOYSA-N 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 3
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- JUWGUJSXVOBPHP-UHFFFAOYSA-B titanium(4+);tetraphosphate Chemical compound [Ti+4].[Ti+4].[Ti+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O JUWGUJSXVOBPHP-UHFFFAOYSA-B 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LSZKGNJKKQYFLR-UHFFFAOYSA-J tri(butanoyloxy)stannyl butanoate Chemical compound [Sn+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O LSZKGNJKKQYFLR-UHFFFAOYSA-J 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- CWHJLNJICCBAOK-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-6-yl)ethyl]silane Chemical group C1CCCC2OC21CC[Si](OC)(OC)OC CWHJLNJICCBAOK-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical group CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 150000003755 zirconium compounds Chemical class 0.000 description 1
- 229910000166 zirconium phosphate Inorganic materials 0.000 description 1
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/06—Preparatory processes
- C08G77/08—Preparatory processes characterised by the catalysts used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
- C08L2203/206—Applications use in electrical or conductive gadgets use in coating or encapsulating of electronic parts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Non-Metallic Protective Coatings For Printed Circuits (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003354122 | 2003-10-14 | ||
| JP2003354122A JP4645793B2 (ja) | 2003-10-14 | 2003-10-14 | 電極回路保護用シリコーンゴム組成物、電極回路保護材及び電気・電子部品 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1621448A CN1621448A (zh) | 2005-06-01 |
| CN100513485C true CN100513485C (zh) | 2009-07-15 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2004100852991A Expired - Fee Related CN100513485C (zh) | 2003-10-14 | 2004-10-14 | 电极电路保护用硅橡胶组合物、电极电路保护材料和电气、电子零件 |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JP4645793B2 (enrdf_load_stackoverflow) |
| KR (1) | KR101092092B1 (enrdf_load_stackoverflow) |
| CN (1) | CN100513485C (enrdf_load_stackoverflow) |
| TW (1) | TW200513498A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106232747A (zh) * | 2014-01-14 | 2016-12-14 | 罗伯特·博世有限公司 | 具有硅聚合物涂层的电路载体 |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006206816A (ja) * | 2005-01-31 | 2006-08-10 | Ge Toshiba Silicones Co Ltd | 室温硬化性ポリオルガノシロキサン組成物 |
| JP4647321B2 (ja) * | 2005-01-31 | 2011-03-09 | モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 | 室温硬化性ポリオルガノシロキサン組成物 |
| JP2006330277A (ja) * | 2005-05-25 | 2006-12-07 | Fuji Xerox Co Ltd | 静電潜像現像剤用キャリア及びその製造方法、静電潜像現像剤、画像形成装置 |
| JP2007161999A (ja) * | 2005-11-17 | 2007-06-28 | Shin Etsu Chem Co Ltd | 圧縮永久歪特性に優れた硬化物を与えるｃｉｐｇ用付加硬化型シリコーン組成物及び該組成物の硬化物の圧縮永久歪低減方法 |
| JP5015476B2 (ja) * | 2006-03-01 | 2012-08-29 | 東レ・ダウコーニング株式会社 | 電極・電気回路の保護剤組成物 |
| WO2009099099A1 (ja) * | 2008-02-07 | 2009-08-13 | Nippon Steel Chemical Co., Ltd. | シリコーン樹脂及びその製造方法並びにこのシリコーン樹脂を含んだ硬化型樹脂組成物 |
| US20130032853A1 (en) * | 2010-04-22 | 2013-02-07 | Nippon Kayaku Kabushiki Kaisha | Silver Anti-Tarnishing Agent, Silver Anti-Tarnishing Resin Composition, Silver Anti-Tarnishing Method, And Light-Emitting Diode Using Same |
| WO2013118752A1 (ja) * | 2012-02-10 | 2013-08-15 | 三菱樹脂株式会社 | カバーレイフィルム、発光素子搭載用基板、及び光源装置 |
| US20160230044A1 (en) * | 2015-02-10 | 2016-08-11 | International Business Machines Corporation | Modified Conformal Coatings With Decreased Sulfur Solubility |
| JP6637674B2 (ja) * | 2015-04-30 | 2020-01-29 | 信越化学工業株式会社 | プリント配線板、プリント配線板の製造方法、及び半導体装置 |
| CN105489418B (zh) * | 2015-12-31 | 2017-09-01 | 宝鸡市晨光真空电器有限责任公司 | 用于户外高压真空断路器的固封式极柱模块的固封工艺 |
| EP4186953A4 (en) * | 2020-07-22 | 2024-08-14 | Shin-Etsu Chemical Co., Ltd. | ANTI-SULFURIZATION COATING MATERIAL, CURED PRODUCT THEREOF, AND ELECTRONIC DEVICE |
| JP2022034356A (ja) * | 2020-08-18 | 2022-03-03 | 信越化学工業株式会社 | ゼオライト含有シリコーンゴム組成物及びその製造方法 |
| JP2024502054A (ja) * | 2020-12-31 | 2024-01-17 | エルケム・シリコーンズ・シャンハイ・カンパニー・リミテッド | 積層造形物体の後処理方法 |
| AT525377B1 (de) * | 2021-08-30 | 2025-02-15 | Hraschan Jakob | Überzug für Oberflächen von Gegenständen aus Holz |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0299641A2 (en) * | 1987-07-17 | 1989-01-18 | Dow Corning Corporation | A curable composition |
| US5276414A (en) * | 1991-12-10 | 1994-01-04 | Mitsubishi Denki Kabushiki Kaisha | Moistureproof structure for module circuits |
| CN1255515A (zh) * | 1998-12-03 | 2000-06-07 | 瓦克化学有限公司 | 用于制备电缆或型材的聚硅氧烷橡胶组合物 |
| CN1282354A (zh) * | 1997-09-16 | 2001-01-31 | Ge拜尔硅股份有限公司 | 加成交联的硅橡胶混合物、其制备方法和其用途 |
| CN1358800A (zh) * | 2000-12-14 | 2002-07-17 | 瓦克化学有限公司 | 可固化的有机聚硅氧烷调制剂 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2560067B2 (ja) * | 1988-03-01 | 1996-12-04 | 第一稀元素化学工業株式会社 | 脱臭剤 |
| JPH03285907A (ja) * | 1990-03-31 | 1991-12-17 | Toshiba Corp | エポキシ樹脂組成物及び樹脂封止型半導体装置 |
| JPH04296046A (ja) * | 1991-03-26 | 1992-10-20 | Toshiba Corp | 樹脂封止型半導体装置 |
| JP2626377B2 (ja) * | 1991-11-05 | 1997-07-02 | 信越化学工業株式会社 | エポキシ樹脂組成物及び半導体装置 |
| JPH0762242A (ja) * | 1993-08-27 | 1995-03-07 | Shin Etsu Chem Co Ltd | 抗菌・抗かび性シリコーンゴム組成物 |
| JP3127093B2 (ja) | 1994-03-03 | 2001-01-22 | 信越化学工業株式会社 | 熱伝導性シリコーンゴム組成物 |
| JPH10155883A (ja) * | 1996-12-02 | 1998-06-16 | Toagosei Co Ltd | 硫黄系悪臭ガス用消臭剤及び消臭性繊維 |
| JPH10277373A (ja) * | 1997-04-04 | 1998-10-20 | Yoshihiko Kanchiku | イオン交換性中空濾過膜およびその製法 |
| JP3444199B2 (ja) | 1998-06-17 | 2003-09-08 | 信越化学工業株式会社 | 熱伝導性シリコーンゴム組成物及びその製造方法 |
| JP4112125B2 (ja) * | 1999-08-13 | 2008-07-02 | 電気化学工業株式会社 | 微細球状シリカ粉末の製造方法 |
| JP2002275446A (ja) * | 2001-03-21 | 2002-09-25 | Showa Denko Kk | 表面実装用接着剤組成物 |
| JP2002371195A (ja) * | 2001-06-18 | 2002-12-26 | Kyocera Chemical Corp | 封止用樹脂組成物および半導体封止装置 |
| JP2002371194A (ja) * | 2001-06-18 | 2002-12-26 | Kyocera Chemical Corp | 封止用樹脂組成物および半導体封止装置 |
| JP2003052800A (ja) * | 2001-08-21 | 2003-02-25 | Toagosei Co Ltd | 硫黄系悪臭の消臭に適した消臭剤組成物 |
| JP4114037B2 (ja) * | 2001-09-25 | 2008-07-09 | 信越化学工業株式会社 | 電気・電子部品の硫化防止又は遅延用シリコーンゴム封止・シール材及び硫化防止又は遅延方法 |
| JP2003138098A (ja) * | 2001-10-30 | 2003-05-14 | Sumitomo Bakelite Co Ltd | エポキシ樹脂組成物及び半導体装置 |
| JP3868272B2 (ja) * | 2001-11-15 | 2007-01-17 | 電気化学工業株式会社 | 球状無機質粉末およびこれを充填した樹脂組成物 |
| JP2003160644A (ja) * | 2001-11-27 | 2003-06-03 | Matsushita Electric Works Ltd | 半導体封止用エポキシ樹脂組成物及び半導体装置 |
| JP2003213083A (ja) * | 2002-01-24 | 2003-07-30 | Nippon Kayaku Co Ltd | エポキシ樹脂組成物及びそれを用いたフレキシブル印刷配線板材料。 |
| JP4189626B2 (ja) * | 2002-03-08 | 2008-12-03 | 信越化学工業株式会社 | 有機ケイ素化合物の精製方法及び硬化性シリコーン組成物 |
| JP2003277579A (ja) * | 2002-03-22 | 2003-10-02 | Nippon Kayaku Co Ltd | 高耐熱エポキシ樹脂組成物及びその硬化物 |
| JP2004115583A (ja) * | 2002-09-24 | 2004-04-15 | Hitachi Chem Co Ltd | 封止用エポキシ樹脂成形材料及び電子部品装置 |
| JP4530137B2 (ja) * | 2003-09-17 | 2010-08-25 | 信越化学工業株式会社 | 精密電子部品封止・シール用オルガノポリシロキサン組成物、精密電子部品の腐蝕防止又は遅延方法、並びに銀含有精密電子部品 |
-
2003
- 2003-10-14 JP JP2003354122A patent/JP4645793B2/ja not_active Expired - Fee Related
-
2004
- 2004-06-25 TW TW093118657A patent/TW200513498A/zh not_active IP Right Cessation
- 2004-10-13 KR KR1020040081642A patent/KR101092092B1/ko not_active Expired - Fee Related
- 2004-10-14 CN CNB2004100852991A patent/CN100513485C/zh not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0299641A2 (en) * | 1987-07-17 | 1989-01-18 | Dow Corning Corporation | A curable composition |
| US5276414A (en) * | 1991-12-10 | 1994-01-04 | Mitsubishi Denki Kabushiki Kaisha | Moistureproof structure for module circuits |
| CN1282354A (zh) * | 1997-09-16 | 2001-01-31 | Ge拜尔硅股份有限公司 | 加成交联的硅橡胶混合物、其制备方法和其用途 |
| CN1255515A (zh) * | 1998-12-03 | 2000-06-07 | 瓦克化学有限公司 | 用于制备电缆或型材的聚硅氧烷橡胶组合物 |
| CN1358800A (zh) * | 2000-12-14 | 2002-07-17 | 瓦克化学有限公司 | 可固化的有机聚硅氧烷调制剂 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106232747A (zh) * | 2014-01-14 | 2016-12-14 | 罗伯特·博世有限公司 | 具有硅聚合物涂层的电路载体 |
| CN106232747B (zh) * | 2014-01-14 | 2019-01-15 | 罗伯特·博世有限公司 | 具有硅聚合物涂层的电路载体 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20050036749A (ko) | 2005-04-20 |
| JP4645793B2 (ja) | 2011-03-09 |
| JP2005120155A (ja) | 2005-05-12 |
| KR101092092B1 (ko) | 2011-12-12 |
| TW200513498A (en) | 2005-04-16 |
| TWI335348B (enrdf_load_stackoverflow) | 2011-01-01 |
| CN1621448A (zh) | 2005-06-01 |
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